Catalog Number

-

Brand Name

Custom Medical Specialties, Inc.

Version/Model Number

CMS-2015BB-NS

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

KKX

Product Code Name

Drape, Surgical

Public Device Record Key

d328bad3-a496-4fe4-b52e-e2fdbabd3de1

Public Version Date

November 08, 2018

Public Version Number

3

DI Record Publish Date

November 21, 2016

Package DI Number

00815849020696

Quantity per Package

50

Contains DI Package

00815849020115

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-